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Quality Assurance Auditor
Quality Assurance AuditorClinLab Staffing • Lancaster, SC, US
Quality Assurance Auditor

Quality Assurance Auditor

ClinLab Staffing • Lancaster, SC, US
11 days ago
Job type
  • Full-time
Job description

QA Auditor

Lancaster, SC

Full-Time, Permanent

Roles and Responsibilities

  • Manage audit planning, scheduling, and execute internal and external audits to assess compliance to the regulations.
  • Audit external suppliers (CMO's) and maintain the vendor qualification program including the Approved Vendor List in Qualityze
  • Manage external vendor(s) responsible for international audits
  • Manage supplier corrective action request program (SCAR).
  • Manage all documents relating to audits, vendors, and suppliers in a QMS (Qualityze)
  • Determine the level of risk of findings identified and follow up on corrective actions ensuring they address the short-term correction as well as the preventive action of the finding.
  • Develop and implement a performance tracking system and reporting of departmental compliance.
  • Prioritize work to ensure that audits and reports are completed in a timely manner. Support implementation of CAPA program where necessary.
  • Train and assist internal departments to understand and comply with Quality and Compliance expectations.
  • Assess internal audit process by identifying and prioritizing areas of the business where there is a risk of non-compliance and assist in development and / or execute processes or policies to reduce that risk.
  • Support training and readiness for regulatory inspections.
  • Provide support to other Quality Assurance team members.
  • Report audit metrics to Quality Assurance and department management.
  • Communicate effectively with all levels of the organization and departments within the organization and function within a team environment.
  • Understand the roles and responsibilities of the Contract Manufacturing Organizations and provide Quality Assurance support for product development, investigations, and CAPAs as required.
  • Familiar with QA functions in SAP.
  • Perform other assigned duties as may be required in meeting Quality Assurance and company objectives.

Minimum Requirements

  • Must have a minimum of 5 years of Quality Assurance auditing experience in cGMP environment with a minimum of 5 years of external vendor / supplier compliance auditing experience within an FDA regulated industry.
  • Knowledge of the Regulations 21CFR Part(s) 210, 211, 507 as well as the Dietary Supplement Regulations 21 CFR 111 is required.
  • ASQ Certified Auditor (CQA) Certification is preferred.
  • Must be proficient in Computer Software applications including MS office suite.
  • Must be able to stand, walk, push, and pull in a variety of environments including a Manufacturing and clean rooms.
  • Must have the ability to wear all required Personal Protective Equipment (PPE) based on the auditing environment.
  • Must be able to travel 20 – 30% for domestic audits, (International travel may be needed per quality management).
  • Education and Experience

    B.A. or B.S. in Science or Technical field required.

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    Quality Auditor • Lancaster, SC, US

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